510(k) K883763 ยท KOD Catheter, Urological
ACME GUIDEWIRES FOR PERCUTANEOUS INSERTION OF CATH
| Applicant | Acme-Monaco Corp., Plainville CT, US |
| Decision | Substantially Equivalent, Nov 18, 1988 |
| Received | Sep 6, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883763
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.